291-15-6 (1,2,4,5-四氧化烷,1,2,4,5-Tetroxane)

快速询单

结构式：

1,2,4,5-四氧化烷MOL文件

CAS号：

291-15-6

中文名称：

1,2,4,5-四氧化烷

英文名称：

1,2,4,5-Tetroxane

分子式：

C₂H₄O₄

分子量：

92.0507612228394

1,2,4,5-四氧化烷(291-15-6)名称与标识符

名称

英文别名：

1,2,4,5-Tetroxane;1,2,4,5-tetraoxane;LogP;291-15-6;DTXSID10467807;CHEMBL2071269;

标识符

InChIKey：

UYVWNPAMKCDKRB-UHFFFAOYSA-N

Inchi：

1S/C2H4O4/c1-3-5-2-6-4-1/h1-2H2

SMILES：

O1COOCO1

1,2,4,5-四氧化烷(291-15-6)物化性质

实验特性

PSA : 36.92

计算特性

精确分子量 : 92.01092
氢键供体数量 : 0
氢键受体数量 : 4
可旋转化学键数量 : 0
同位素质量 : 92.01095860g/mol
重原子数量 : 6
复杂度 : 26.5
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : 0
拓扑分子极性表面积 : 36.9Å²

1,2,4,5-四氧化烷(291-15-6)相关文献

1. Synthetic methods for unsymmetrically-substituted 1,2,4,5-tetroxanes and of 1,2,4,5,7-pentoxocanes
Hye-Sook Kim,Kaoru Tsuchiya,Yasuharu Shibata,Yusuke Wataya,Yoshihiro Ushigoe,Araki Masuyama,Masatomo Nojima,Kevin J. McCullough J. Chem. Soc. Perkin Trans. 1 1999 1867
2. The synthesis, X-ray structural analysis, and anomeric effect in trans-3,6-dimethoxy-1,2,4,5-tetroxane
Chin-Yun Chiang,William Butler,Robert L. Kuczkowski J. Chem. Soc. Chem. Commun. 1988 465
3. The synthesis, X-ray structural analysis, and anomeric effect in trans-3,6-dimethoxy-1,2,4,5-tetroxane
Chin-Yun Chiang,William Butler,Robert L. Kuczkowski J. Chem. Soc. Chem. Commun. 1988 465
4. Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
D. V. Kazakov,A. R. Timerbaev,F. E. Safarov,T. I. Nazirov,O. B. Kazakova,G. Y. Ishmuratov,A. O. Terent'ev,D. A. Borisov,A. G. Tolstikov,G. A. Tolstikov,W. Adam RSC Adv. 2012 2 107
5. Second generation analogues of RKA182: synthetic tetraoxanes with outstanding in vitro and in vivoantimalarial activities
Francesc Marti,James Chadwick,Richard K. Amewu,Hollie Burrell-Saward,Abhishek Srivastava,Stephen A. Ward,Raman Sharma,Neil Berry,Paul M. O'Neill Med. Chem. Commun. 2011 2 661
6. Synthesis of some novel steroidal 1,2,4,5-tetraoxanes
Archana M. Das,Manash P. Hazarika RSC Adv. 2015 5 19818
7. Design and synthesis of orally active dispiro 1,2,4,5-tetraoxanes; synthetic antimalarials with superior activity to artemisinin
Richard Amewu,Andrew V. Stachulski,Stephen A. Ward,Neil G. Berry,Patrick G. Bray,Jill Davies,Gael Labat,Livia Vivas,Paul M. O'Neill Org. Biomol. Chem. 2006 4 4431
8. Identification of ozonides by oxygen-17 NMR spectroscopy
J. Lauterwein,K. Griesbaum,P. Krieger-Beck,V. Ball,K. Schlindwein J. Chem. Soc. Chem. Commun. 1991 816
9. Synthesis and reaction of 1,2,4-trioxanes
Tomohiro Fujisaka,Masahiro Miura,Masatomo Nojima,Shigekazu Kusabayashi J. Chem. Soc. Perkin Trans. 1 1989 1031
10. Chair–chair interconversion in some highly substituted 1,2,4-trioxanes and 1,3-dioxanes. A dynamic NMR study of a striking effect of skeletal substitution
J. Edgar Anderson,A. J. Bloodworth,Aneela Shah J. Chem. Soc. Perkin Trans. 2 1993 1927